Manager, Early Phase Risk & Compliance ParexelManager, Early Phase Risk & ComplianceGlendale, California$120,000–$140,000 / yearAs a Manager, Early Phase Risk and Compliance, you will lead and manage Risk and Compliance Leads who support Early Phase Clinical Units, driving strategic initiatives that enhance quality and ensure compliance with regulatory requirements, client expectations, and internal policies. With 22,000+ employees worldwide, we partner with biopharmaceutical companies and research sites to design and deliver patient-focused clinical trials that broaden access and make research a care option for anyone, anywhere.
Associate Director, Collaborative Operations for Health Engagement. Representation, and Enrollment (COHERE) - West Coast BeOne Medicines AGAssociate Director, Collaborative Operations for Health Engagement. Representation, and Enrollment (COHERE) - West CoastCARemote$143,300–$193,300 / yearWorking cross-functionally across Global Clinical Operations (GCO), Clinical Development, Regulatory, Medical Affairs, Corporate Affairs, and other relevant functions, the Associate Director will help embed patient access considerations into study planning and execution while building trusted relationships with research sites, healthcare institutions, community organizations, and other external stakeholders. The role will leverage data, patient journey insights, site capabilities, and external partnerships to identify and address barriers to clinical trial participation and support informed patient access to BeOne clinical research.
Regulatory Coordinator UCLA Health SystemRegulatory CoordinatorLos Angeles, CA$31.51–$62.64 / hourInterpersonal skills to effectively communicate information in a timely, professional manner and establish and maintain cooperative and effective working relationships with students, staff, faculty, external collaborators and administration and to work as a member of a team. As a condition of employment, the final candidate who accepts an offer of employment will be required to disclose if they have been subject to any final administrative or judicial decisions within the last seven years determining that they committed any misconduct; or have filed an appeal of a finding of substantiated misconduct with a previous employer.
Budget Amendment Negotiator - HematologyOncology Fully Remote UCLA Health SystemBudget Amendment Negotiator - HematologyOncology Fully RemoteCARemote$31.51–$62.64 / hourInterpersonal skills to effectively communicate information in a timely, professional manner and establish and maintain cooperative and effective working relationships with students, staff, faculty, external collaborators and administration and to work as a member of a team. Perform detailed review of clinical research protocols and utilizes that information to prepare, manage and submit all required study/regulatory documents and all required applications and forms related to internal UCLA requirements, FDA requirements, sponsor requirements, etc.
Manager, Quality Parexel International CorpManager, QualityGlendale, CA$135,000–$140,000 / yearAs a Manager, Early Phase Risk and Compliance, you will lead and manage Risk and Compliance Leads who support Early Phase Clinical Units, driving strategic initiatives that enhance quality and ensure compliance with regulatory requirements, client expectations, and internal policies. With 22,000+ employees worldwide, we partner with biopharmaceutical companies and research sites to design and deliver patient-focused clinical trials that broaden access and make research a care option for anyone, anywhere.
Physician Investigator Opportunities - Multiple Locations Nationwide Headlands ResearchPhysician Investigator Opportunities - Multiple Locations NationwideRolling Hills Estates, CAThis general interest posting is designed for physicians who may not see a current opening that perfectly aligns with their location or specialty-but who would like to be considered for future Investigator, Sub-Investigator, or Physician leadership opportunities across our growing network of clinical research sites nationwide. Our physicians play a critical role in advancing innovative therapies, improving patient access to clinical trials, and shaping high-quality, patient-centered research environments.
Quality Assurance Coordinator - Hybrid University of California, IrvineQuality Assurance Coordinator - HybridOrange, CaliforniaFull timeResponsibilities: The Quality Assurance Coordinator conducts and assists with internal quality assurance monitoring and auditing activities for assigned clinical research studies at all participating sites under the CFCCC for the overall review of regulatory, subject management, data compliance, and Investigational Drug Service/Pharmacy research activities under the direction of the Quality Assurance Officer. *Misconduct Disclosure Requirement: As a condition of employment, the final candidate who accepts a conditional offer of employment will be required to disclose if they have been subject to any final administrative or judicial decisions within the last seven years determining that they committed any misconduct; received notice of any allegations or are currently the subject of any administrative or disciplinary proceedings involving misconduct; have left a position after receiving notice of allegations or while under investigation in an administrative or disciplinary proceeding involving misconduct; or have filed an appeal of a finding of misconduct with a previous employer.
Implementation Manager (bilingual) CRIO IncImplementation Manager (bilingual)CAYou'll be the first point of contact for our newest clients post-sale and provide an overview of the onboarding project, set up recurring calls/trainings with critical stakeholders at the client level, and collaborate with other CRIO teams/departments to help expand and optimize the capacity of the team. Founded in 2015 by a clinical trial site owner seeking to improve his own business, today CRIO is the industry leader in site eSource with a fast-growing presence serving sponsors and CROs.
CRC Asst University of California, IrvineCRC AsstOrange, CaliforniaFull timeSpecific responsibilities and key duties involve screening, recruitment, scheduling and retention of study participants, collection of psychological, behavioral, biological and clinical data at study visits, abstraction of data from medical records, management of research databases, isolation and culture of stem cells from newborn blood and tissues, processing and storage of biospecimens (e.g., blood, saliva, urine), conducting infant non-invasive scans/phenotyping (e.g., skinfold, anthropometric measurements, PeaPod, magnetic resonance imaging scans (MRI)), and management and ordering of research supplies for the clinical and laboratory spaces. Accordingly, the Clinical Research Coordinator is responsible for the day-to-day implementation, coordination, and oversight of human subjects study activities, including participant screening, recruitment and retention, informed consent, study visits, data management, regulatory compliance, and study logistics, and is additionally responsible for laboratory management including biospecimen collection and processing, and laboratory supply and equipment management.
Principal, Clinical Programming, Surgical Edwards Lifesciences CorpPrincipal, Clinical Programming, SurgicalIrvine, CA$132,000–$186,000 / yearHow you will make an impact: Provide technical expertise in clinical programming functional area and lead in the development of clinical databases, and tools and programs for data validation checks, and clinical trial reporting in collaboration with key stakeholders. Lead cross functional teams in the design and delivery of complex functional modules and provide clinical programming expertise regarding clinical trials, protocols, and case report forms.
Senior Analyst, Clinical Data Management Edwards LifesciencesSenior Analyst, Clinical Data ManagementIrvine, CaliforniaLeading project management activities for multiple (multi-site and multi-cohort) projects to bring clinical studies on-line, including conducting project team meetings, establishing and maintaining project timelines, and communications to stakeholders. Defining and specifying clinically complex data collection requirements (e.g., eCRFs, CRFs, edit checks and collection of external data) for assigned studies; including defining, performing, and coordinating user acceptance testing (e.g.
Medical Assistant/Patient Services Representative Children's Hospital Los AngelesMedical Assistant/Patient Services RepresentativeArcadia, California$47,840–$63,024 / yearFull timePurpose Statement/Position Summary: The Medical Assistant/Patient Services Representative provides patient-families with a positive experience at CHLA by performing a variety of patient care and clerical activities to assist physicians, nursing and clerical personnel. Children’s Hospital Los Angeles is consistently ranked among the top 10 children's hospitals in the nation, delivering world-class care through more than 350 specialized programs and services.
Nurse Supervisor, Oncology Flourish ResearchNurse Supervisor, OncologyCentury City, California$75–$90 / hourServes as a lead infusion nurse, including performing IV infusions, and/or injections of blinded and unblinded study drugs, obtaining blood specimens, and maintaining accurate source documentation. Perform IV infusion and IM/SQ injections of blinded and unblinded investigational products according to study protocols, Obtain blood specimens and other biological samples from study participants/patients following proper clinical procedures.
Client Executive Advarra IncClient ExecutiveCA$95,000–$175,000 / yearRepresent relevant Advarra services offerings across services and product / technology and partner with other Advarra business units to ensure penetration of Advarra's services and products into our customers. Treating one another, our clients, and clinical trial participants with empathy and care are key tenets of our culture at Advarra; we are committed to creating a workplace where each employee is not only valued but empowered to thrive and make a meaningful impact.
Clinical Scientist / Neuropsychological Rater (Bilingual Mandarin) Irvine Center for Clinical Research IncClinical Scientist / Neuropsychological Rater (Bilingual Mandarin)Irvine, CA$80,000–$90,000 / yearEmpirical Case Building & Advocacy: Synthesize diagnostic data and clinical history to build objective, evidence-based cases for protocol eligibility, advocating for complex or nuanced candidates who qualify under protocol criteria. Preferred Experience: Prior psychometrician or clinical rater experience in pharmaceutical clinical trials (specifically in Alzheimer's Disease, MCI, or Major Depressive Disorder) is preferred and qualifies for higher starting compensation.
Clinical Training & Educational Specialist BiVACORClinical Training & Educational SpecialistHuntington Beach, CaliforniaThis is a high-impact, creative role at the intersection of clinical science and education, where your expertise will directly shape how investigational site teams around the world learn to support patients receiving the BiVACOR Total Artificial Heart. You will bring instructional design expertise, a collaborative mindset, and a passion for translating complex clinical and technical concepts into clear, effective learning experiences.
Clinical Trials Data Coord City of HopeClinical Trials Data CoordDuarte, CARemoteCity of Hope's growing national system includes its Los Angeles campus, a network of clinical care locations across Southern California, a new cancer center in Orange County, California, and treatment facilities in Atlanta, Chicago and Phoenix. Collaborate effectively as a valuable member of the clinical research team, demonstrating clear and timely written and verbal communication skills, including the sharing of critical information.
Physician | GU Medical Oncologist | COHOC (Irvine, CA) City of HopePhysician | GU Medical Oncologist | COHOC (Irvine, CA)Irvine, CA$400,000–$550,000 / yearCity of Hope's growing national system includes its Los Angeles campus, a network of clinical care locations across Southern California, a new cancer center in Orange County, California, and cancer treatment centers and outpatient facilities in the Atlanta, Chicago and Phoenix areas. With an independent, National Cancer Institute-designated comprehensive cancer center that is top ranked in the nation for cancer care by U.S. News & World Report at its core, City of Hope's uniquely integrated model spans cancer care, research and development, academics and training, and a broad philanthropy program that powers its work.
Clinical Athletic Trainer Children's Hospital Los AngelesClinical Athletic TrainerLos Angeles, CARemotePurpose Statement/Position Summary: The primary role of the Clinical Athletic Trainer (ATC) is to assist in the examination and treatment of patients under the direction of the physician and/or Sports Medicine Program manager by performing the essential functions of the job. The position will collaborate with multi-disciplinary team and provide direct assistance to other medical providers such as physicians, advanced practice providers, physical therapists, medical assistants, and registered nurses in providing care for our patients at CHLA.
Senior Administrative Assistant Children's Hospital Los AngelesSenior Administrative AssistantLos Angeles, California$52,728–$70,304 / yearFull timeIntegrated Delivery Systems (IDS) designs and supports innovative care models that integrate medical, social, and community-based services to improve health outcomes, reduce disparities, and deliver seamless, family-centered care across Children's Hospital Los Angeles. Children’s Hospital Los Angeles is consistently ranked among the top 10 children's hospitals in the nation, delivering world-class care through more than 350 specialized programs and services.